Non-synonymous FBXW7 Gene Mutation

Preferred Label : Non-synonymous FBXW7 Gene Mutation;

NCIt synonyms : FBXW7 Missense Mutation; Non-synonymous F-Box and WD Repeat Domain Containing 7 Gene Mutation; Non-synonymous CDC4 Gene Mutation; Non-synonymous FBW6 Gene Mutation; Non-synonymous FBW7 Gene Mutation; Non-synonymous SEL10 Gene Mutation; Non-synonymous FBXW6 Gene Mutation; Non-synonymous Archipelago Homolog, Drosophila Gene Mutation; FBXW7 Missense Gene Mutation; Non-synonymous AGO Gene Mutation; Non-synonymous SEL-10 Gene Mutation; Non-synonymous F-box and WD-40 Domain Protein 7 (Archipelago Homolog, Drosophila) Gene Mutation; Non-synonymous FBX30 Gene Mutation; Non-synonymous Archipelago Homolog Gene Mutation;

NCIt definition : A point mutation in the FBXW7 gene that encodes an amino acid substitution in the F-box/WD repeat-containing protein 7 protein.;

NCI Metathesaurus CUI : CL950769;

Details

Origin ID

C158678;

UMLS CUI

C5203877;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
molecular_abnormality_involves_gene
- FBXW7 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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